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"LICAR" Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 9dddd61a8c7719e535211ab0a53b3613

Access comprehensive regulatory information for "LICAR" Corrective Spectacle Lens (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9dddd61a8c7719e535211ab0a53b3613 and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is SHENG MAO OPTICAL CO., LTD..

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9dddd61a8c7719e535211ab0a53b3613
Registration Details
Taiwan FDA Registration: 9dddd61a8c7719e535211ab0a53b3613
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Device Details

"LICAR" Corrective Spectacle Lens (Non-Sterile)
TW: "็”Ÿ่Œ‚" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9dddd61a8c7719e535211ab0a53b3613

Ministry of Health Medical Device Import No. 018445

DHA09401844505

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Oct 24, 2017

Oct 24, 2022